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1 rhythmias among RAFT study participants were downloaded and adjudicated by 2 blinded reviewers with an overreader for dis
4 asured by flow cytometry, and prevalent diabetes cases were adjudicated by 2 physicians for PWH and HIV-negative particip
7 defined as hospitalization for ADHF, confirmed and formally adjudicated by a blinded events committee using standardized
8 mic stroke, and hospitalization for heart failure (HF) were adjudicated by a blinded events committee.
9 All serious adverse events including deaths were adjudicated by a blinded, third-party, independent Clinical E
16 "liver-related," "non-liver-related," and "non-descript" as adjudicated by a panel comprised of a transplant surgeon, a h
17 s 'liver related', 'nonliver related', and 'nondescript' as adjudicated by a panel comprised of a transplant surgeon, a h
23 e no device- or procedure-related deaths in either group as adjudicated by an independent and blinded Clinical Events Com
25 ined with Valve Academic Research Consortium 2 criteria and adjudicated by an independent clinical events committee.
27 ence, or death (all-cause), from randomisation to 12 weeks, adjudicated by an independent review committee masked to the
29 were followed up for incident cancer diagnoses, which were adjudicated by an oncology endpoint committee masked to drug
30 Appropriateness of antibiotic use was adjudicated by at least 2 infectious diseases-trained clinici
31 y outcome was proven or probable invasive fungal disease as adjudicated by blinded central review.
32 Medical records were sought for potential cases and adjudicated by board-certified pediatricians.
33 Overall, 89 patients (2%) had major bleeding adjudicated by clinician review, with 27 of 900 (3.0%) on the
39 t A (1205 images, 1 image/patient; 18.1% referable), images adjudicated by panels of GSs; dataset B (9642 images, 1 image
46 transplantation, prediction of wait-list (WL) mortality is adjudicated by the Model for End Stage Liver Disease-Sodium (